MIR1282 microRNA 1282 [Homo sapiens (human)] - Gene

Summary

Official Symbol: MIR1282provided by HGNC
Official Full Name: microRNA 1282provided by HGNC
Primary source: HGNC:HGNC:35360
See related: Ensembl:ENSG00000221792 miRBase:MI0006429; AllianceGenome:HGNC:35360
Gene type: ncRNA
RefSeq status: PROVISIONAL
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: MIRN1282; hsa-mir-1282
Summary: microRNAs (miRNAs) are short (20-24 nt) non-coding RNAs that are involved in post-transcriptional regulation of gene expression in multicellular organisms by affecting both the stability and translation of mRNAs. miRNAs are transcribed by RNA polymerase II as part of capped and polyadenylated primary transcripts (pri-miRNAs) that can be either protein-coding or non-coding. The primary transcript is cleaved by the Drosha ribonuclease III enzyme to produce an approximately 70-nt stem-loop precursor miRNA (pre-miRNA), which is further cleaved by the cytoplasmic Dicer ribonuclease to generate the mature miRNA and antisense miRNA star (miRNA*) products. The mature miRNA is incorporated into a RNA-induced silencing complex (RISC), which recognizes target mRNAs through imperfect base pairing with the miRNA and most commonly results in translational inhibition or destabilization of the target mRNA. The RefSeq represents the predicted microRNA stem-loop. [provided by RefSeq, Sep 2009]
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Genomic context

Location:: 15q15.3

Exon count:: 1

Annotation release	Status	Assembly	Chr	Location
RS_2023_10	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (43793659..43793759, complement)
RS_2023_10	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (41601022..41601122, complement)
105.20220307	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (44085857..44085957, complement)

Chromosome 15 - NC_000015.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Submit: New GeneRIF Correction

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

General gene information

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Markers

REN37696 (e-PCR)
- UniSTS:362496

REN37697 (e-PCR)
- UniSTS:362497

REN37698 (e-PCR)
- UniSTS:362498

REN37699 (e-PCR)
- UniSTS:362499

ECD04146 (e-PCR)
- UniSTS:285224

ECD03905 (e-PCR)
- UniSTS:284985

RH41787 (e-PCR)
- UniSTS:49500

D15S797 (e-PCR)
- UniSTS:151794

REN37689 (e-PCR)
- UniSTS:362489

REN37690 (e-PCR)
- UniSTS:362490

REN37691 (e-PCR)
- UniSTS:362491

REN37692 (e-PCR)
- UniSTS:362492

REN37693 (e-PCR)
- UniSTS:362493

REN37694 (e-PCR)
- UniSTS:362494

REN37695 (e-PCR)
- UniSTS:362495

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.